SPINAL STABILIZING SPHERE SYSTEM— 510(k) K063139

Unknown

Biomet Spine

FDA 510(k) clearance K063139 for SPINAL STABILIZING SPHERE SYSTEM, Unknown on 2007-04-04. Applicant: Biomet Spine. Device class: 3.

Clearance details

Applicant: Biomet Spine
Product code: Code NVR
Device class: Class 3
Advisory panel: Unknown
Date received: 2006-10-16
Decision date: 2007-04-04
Decision: Unknown
Clearance type: Traditional
Location: Warsaw, IN, US

Download summary PDF View on FDA.gov ↗

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K060415 — MODIFICATION TO: SATELLITE SPINAL SYSTEM2007-01-05
K051320 — SATELLITE SPINAL SYSTEM2005-09-09

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Data sourced from openFDA. This site is unofficial and independent of the FDA.